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Prion protein inhibits fast axonal transport through a mechanism involving casein kinase 2
Prion diseases include a number of progressive neuropathies involving conformational changes in cellular prion protein (PrP(c)) that may be fatal sporadic, familial or infectious. Pathological evidence indicated that neurons affected in prion diseases follow a dying-back pattern of degeneration. How...
Autores principales: | Zamponi, Emiliano, Buratti, Fiamma, Cataldi, Gabriel, Caicedo, Hector Hugo, Song, Yuyu, Jungbauer, Lisa M., LaDu, Mary J., Bisbal, Mariano, Lorenzo, Alfredo, Ma, Jiyan, Helguera, Pablo R., Morfini, Gerardo A., Brady, Scott T., Pigino, Gustavo F. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737884/ https://www.ncbi.nlm.nih.gov/pubmed/29261664 http://dx.doi.org/10.1371/journal.pone.0188340 |
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